A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319554



Internal ID20852649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32079857..32107225hg38UCSC Ensembl
chr1:32545458..32572826hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3827369
hg1927369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203594
Samples
Known GenesTMEM39B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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